Key result
Hyperlactatemia in sepsis survivors is linked to ~54% higher long-term all-cause mortality.
Cohort (n=2,285)
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Randomized trial investigates long-term risks of mortality and cardiovascular events in sepsis survivors with hyperlactatemia, suggesting urgent management may be needed.
INTRODUCTION: Serum lactate is a potentially valuable biomarker for risk assessment for patients with sepsis, as hyperlactatemia is associated with elevated short-term mortality risks. However, the associations between hyperlactatemia and long-term clinical outcomes in sepsis survivors remain unknown. The objective of this study was to investigate whether hyperlactatemia at the time of hospitalisation for sepsis was associated with worse long-term clinical outcomes in sepsis survivors. METHODS: = 2285) lactate groups. The high lactate group was then matched 1:1 by propensity-score method to the low lactate group. The outcomes of interest were all-cause mortality, major adverse cardiac events (MACEs), ischaemic stroke, myocardial infarction, hospitalisation for heart failure, and end-stage renal disease. RESULTS: After propensity score matching, the high lactate group had greater risks of all-cause mortality (hazard ratio [HR] 1.54, 95% confidence interval [CI] 1.41-1.67), MACEs (HR 1.53, 95% CI 1.29-1.81), ischaemic stroke (HR 1.47, 95% CI 1.19-1.81), myocardial infarction (HR 1.52, 95% CI 1.17-1.99), and end-stage renal disease (HR 1.42, 95% CI 1.16-1.72). Subgroup analyses stratified by baseline renal function revealed almost similarity across groups. CONCLUSION: We found that hyperlactatemia is associated with long-term risks of mortality and MACEs in sepsis survivors. Physicians may consider more aggressive and prompter management of sepsis in patients who present with hyperlactatemia to improve long-term prognoses.
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Ou et al. (2023) conducted a cohort in Sepsis (n=2,285). Hyperlactatemia (high lactate) vs. Low lactate was evaluated on All-cause mortality (HR 1.54, 95% CI 1.41-1.67). Hyperlactatemia in sepsis survivors was associated with increased risks of long-term all-cause mortality (HR 1.54; 95% CI 1.41-1.67) and MACE (HR 1.53; 95% CI 1.29-1.81).
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